Lab 3 Guide: Gas Chromatography (GC) (Sept 8-14)
How GC works – The Basic Idea
Gas chromatography (GC) is mainly used for the qualitative analysis of samples: it answers
the question “What chemicals are present in this sample, and in what relative proportions?”
The basic idea is that you inject a liquid into a long coil (or column) which is contained in
an oven. Because oven heats the coil the liquid will vaporize. Because the coil is long it will
take the vapors some time to reach the end of the coil.
Different vapors will exit the coil at different times. We can compare these times to
standard values to determine the identity of the vapors, and therefore, the chemicals that
were in the sample.
How GC works – The Details
Every form of chromatography uses both a mobile phase and a stationary phase.
In GC the mobile phase is an inert (non-reactive) gas such as nitrogen or helium.
The stationary phase is a non-volatile liquid that coats the inside of the column. An
example is polyethylene glycol (PEG).
Let’s say you want to run a GC on a sample which is two-parts ethanol and one-part 1propanol by volume. You would inject a very small amount of the sample into the columnabout 1 micro liter (uL; 1/1000 of a mL).
The boiling point of ethanol is 80 ºC and the boiling point of 1-propanol is 97 ºC, so a good
temperature for the oven is 88 ºC- the average of their boiling points.
After injection the liquid would evaporate and the vapors would dissolve in the liquid
coating the column (the stationary phase).
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Lab 3 Guide: Gas Chromatography (GC) (Sept 8-14)
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The carrier gas (mobile phase) would push these vapors through the length of the column,
at which point they would register with a detector. The time is takes to travel through a
column is called the retention time (Rt).
In general, the higher the boiling point of a liquid, the higher its retention time.
So we would expect the ethanol to “come off the column” the first and then the 1-propanol;
the ethanol would have a shorter retention time than the 1-propanol.
This would be recorded as a two peaks. The area of each peak is proportional to the amount
of chemical present in the sample. Because we have twice as much ethanol as 1-propanol,
the integration of the ethanol peak should be twice that of the 1-propanol peak.
Key GC Concepts
Factors that affect resolution, retention times, and peak shape
The term resolution refers to well separated two peaks are from each other.
If two peaks are so close together that you can’t tell when one peak begins and the other
ends the resolution is poor; you can also say that the separation is poor. If you can clearly
identify two different peaks the resolution is good.
The longer and more narrow the column, the better the resolution.
Lab 3 Guide: Gas Chromatography (GC) (Sept 8-14)
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Increasing the carrier gas flow rate and/or the temperature will send the vapors through the
column faster, which will lower the retention time and worsen the resolution. Lowering the
temperature and/or flow rate increases retention times and broadens the peaks.
Solubility and the mobile phase
It’s important that the chemicals you wish to analyze are soluble in the mobile phase of
your column. Otherwise, you won’t get a good separation.
Remember the rule “like dissolves like”. For example, if you want to run a GC on octane,
which is non-polar, silicone oil is a suitable mobile phase because it is also non-polar. But
for a polar chemical such as an alcohol, a polar mobile phase such as polyethylene glycol
(PEG) should be used instead.
Air to mark time zero
Right after the injection your TA will probably run a small amount of air through the column.
This marks a retention time of zero on the GC print out.
Lab 3 Guide: Gas Chromatography (GC) (Sept 8-14)
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Attenuation
To attenuate is to weaken. If the amplitude (height) of the peaks on your GC print out are
too high your TA will increase the attenuation settings of the GC, which will lower the peak
amplitude and the sensitivity of the detector.
Conversely, if the sensitivity of the GC is so low that nothing registers with the detector, the
right move is to decrease the attenuation settings.
What do peak integrations really tell us?
Peak integrations tell us the relative amounts of each chemical present, not the exact
amounts. This is because different chemicals will respond differently to the detector.
Accurate quantitative analysis is possible using GC, but you would first need to calibrate
the instrument. (i.e. a calibrated 2:1 methanol-ethanol mixture gives a 2.132:1.091 peak
integration ratio, etc.)
How Detectors Work
You should probably know how the chemicals are registered at two common types of
detectors.
A thermal conductivity detector uses a material that changes its electrical resistance with
varying temperatures. Helium is very good at transferring heat. Most other gases are not. So
when a sample comes off the column, the temperature at the detector will suddenly drop.
This causes a change in the electrical voltage, which registers with the detector.
A flame ionization detector burns the sample as it comes off the column. This creates ions
that produce an electrical current, which registers with the detector. An advantage of this
method is that you don’t need to use helium gas, which is expensive. Nitrogen can be used
instead.
Plain English Procedure
There’s not much of a procedure for this lab. You will stand with your TA as he or she runs
GCs for several known alcohols. Then the TA will run a GC on an unknown sample, which is
some combination of alcohols.
Based on the retention time and peak integrations from the unknown sample GC you can
determine what alcohols are present in the sample.
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For example, let’s say the retention times of methanol and 1-propanol are 3.04 and 5.42
minutes, respectively. If your unknown sample has two retention times of 2.96 and 5.51
minutes, then your unknown contains methanol and 1-propanol (the retention times won’t
be exactly the same).
The ratio of peak integrations tells you the relative amounts of methanol and 1-propanol by
volume.
It’s important to do all of your samples consecutively using the same GC. If you run a
sample and then wait 30 minutes the air flow or temperature of the GC might have changed,
which will alter your retention times.
Questions You Will Probably Be Asked
Q: A student is trying to do a GC but his peaks are too short and the resolution is awful.
How can these problems be fixed?
A: The resolution is poor because either the temperature and/or the flow rate is too high;
they should be lowered.
To make the peaks taller decrease the attenuation settings.
(Note: don’t ever mess with the GC settings! Ask your TA!)
Q: A student runs a GC of the same sample on two different GCs. Will the results be the
same?
A: No. Factors such oven temperature, carrier gas flow rate, column length and diameter,
and the type of mobile phase all influence retention times.
And that’s it for this week.